US3772435A

US3772435A - Method of using steroid acetonides as growth promoting agents

Info

Publication number: US3772435A
Application number: US00195040A
Authority: US
Inventors: R Wilbur
Original assignee: American Cyanamid Co
Current assignee: Wyeth Holdings LLC
Priority date: 1971-11-02
Filing date: 1971-11-02
Publication date: 1973-11-13
Anticipated expiration: 1990-11-13

Abstract

ENCHANCEMENT OF THE GROWTH RATE OF FEMALE RUMINANT ANIMALS BY PARENTERALLY ADMINSTERING TO SAID ANIMALS, IN A SINGLE DOSE, A GROWTH-ENCHANCING AMOUNT OF A SELECTED DERIVATIVE OF CERTAIN HALOGENATED 16A, 17A-DIHYDROXYSTEROIDS OF THE PREGNANE SERIES.

Description

United States Patent Oflice 3,772,435 Patented Nov. 13, 1973 METHOD OF USING STEROID ACETONIDES AS GROWTH PROMOTING AGENTS Robert Daniel Wilbur, Titusville, N.J., assignor to American Cyanamid Company, Stamford, Conn. No Drawing. Filed Nov. 2, 1971, Ser. No. 195,040 Int. Cl. A61k 17/00 US. Cl. 424-241 9 Claims ABSTRACT OF THE DISCLOSURE Enchancement of the growth rate of female ruminant animals by parenterally administering to said animals, in a single dose, a growth-enchancing amount of a selected derivative of certain halogenated 16u,17a-dihydroxysteroids of the pregnane series.

DESCRIPTION OF THE INVENTION This invention relates to a method of enchancing the growth rate of female ruminant animals. More particularly, the invention involves parenterally administering to said animals a growth-enchancing composition of a compound having the formula:

CHzCl where R is a member selected from the group consisting of hydrogen, chlorine or fluorine and a pharmaceutically acceptable carrier.

The compound 9a,11p,21-trichloro-16a,17a-(isopropylidenedioxy)-1,4,6-pregnatriene-3,20-dione (R=hydrogen) and method for its preparation is disclosed in United States Patent No. 3,211,727. According to the patent, the compound is a highly effective anti-inflammatory agent. Recently it has also been found that said compound and derivatives thereof are useful as anti-fertility agents (US. Patent 3,608,076) when orally administered to warmblooded females.

The compounds 6,9u,l15,21-tetrachloro-lGo na-(isopropylidenedioxy)-1,4,6-pregnatriene-3,20-dione and 9a, 1113,2l-trichloro-6-fiuoro 16a,17a (isopropylidenedioxy)-1,4,6-pregnatriene 3,20 dione are disclosed in United States Patent No. 3,541,086.

The patentees indicate that such compounds are also anti-inflammatory agents; however, reference to their use as anti-fertility agents is not made. Surprisingly, it has been found that these compounds and their previously mentioned 6-hydrogen analogue are highly effective growth-promoting agents for ruminant female animals, such as, for example, cattle, sheep and goats, when they are parenterally administered to said animals in a single, 100 mg. to 600 mg., dose. It has been also observed that each of said compounds is effective as an anti-fertility agent.

In accordance with the present invention, the active steroid component can be dissolved or dispersed in a pharmaceutically acceptable carrier for use as an injectable solution or suspension. Among the carriers which may be used are (1) the natural triglycerides, such as glycerol, sesame oil, peanut oil, soybean oil, and the like (2) polyhydric alcohols, such as propylene glycol and polyethylene glycols having an average molecular weight between about 200 and 600, and aqueous solutions thereof, (3) saline suspensions generally containing about 0.9% salt, and (4) saline-polyethylene glycol-carbowax solutions. Generally about 100 mg. to 600 mg. of the active compound is dissolved or dispersed in about 5 ml. to 15 ml. of a pharmaceutically acceptable carrier in solution for use as a single injection. Where desired, pH may be adjusted to 6 to 8 with an appropriate acid or base.

While the preferred route of administration of the growth-promoting compounds is via a liquid injection, the compounds can also be prepared and utilized as implants: for example, solid, paste or as a silastic implant.

Examples of formulations that could be used are as follows:

Liquid: Preferred formulation Steroid (100 mg. to 600 mg.) mg 200 Polysorbate percent 0.2 Polyethylene glycol 4000 do 3.0 Benzyl alcohol do.. 0.9 Sodium chloride do 09 Waterq.s. do 100.0

Solid:

Steroid (60% to do 70 Lubricant (i.e. magnesium stearate) do Starchq.s.

Steroid (60% to 90%) do 70 Polyethylene glycol 4000 (3 to 15) do 10 White waxq.s.

Paste:

Drug mg. to 600 mg.) "mg-.. 200 Polyethylene glycol 4000' (30% to 50%) percent.. 40

Polyethylene glycol 400-q.s.

Moreover, such compounds can also be used as growthpromoting agents in combination with other growthpromoting drugs, such as diethylstilbestrol.

SPECIFIC DISCLOSURE The invention is further illustrated by the examples set forth below. Parts are by weight unless otherwise indicated.

EXAMPLE 1 In the following test, purebred Hereford heifers, approximately 15 months of age, were used. Each heifer received a full feed (approximately 18 kg.) of corn silage each morning and 2.3 kg. of a high roughage pelleted diet every evening. The diet used contained the following: Ingredient: Percent Ground corn cobs 40.0 Ground yellow corn 32.0 Dehydrated alfalfa meal (17%) 15.0

Soybean oil meal (44%) 2.5 Cane molasses 7.0 Urea (45% -N) 1.0 Dicalcium phosphate 1.5 Trace mineralized salt 1.0 Total 100.0

Fortified with 909 LU. Vitamin A and 227 LU. Vitamin D per kilogram.

Fresh water was supplied ad libitum.

Each heifer selected for use in this test had exhibited three or more normal 18 to 22-day estrus cycles. The quantity of test compound to be injected into each heifer was weighed out into a 10 ml. serum vial. Within an hour before injection, 5 ml. sesame oil was added and the contents were vigorously mixed on a Vortex Jr. mixer for 5 minutes. This mixture was then drawn up into a ml; syringe through a 19 gauge 1.5-inch long needle and injected into the right triceps muscle. The vial was rinsed twice with additional 5 ml. aliquots of sesame oil, which were drawn into the same syringe and injected into the same muscle. Control animals were injected in the same manner with sesame oil only. All compounds were injected at approximately 1:15 pm. on the scheduled day of injection, which was 7 days prior to the next expected estrus (estimated at 20 days from the last behavioral estrus). Each of six heifers in four groups received 0, 50, 100, or 200 mg. of the test compound 9a,1l}3,2l-trich1orol6a,l7a (isopropylidenedioxy)-1,4,6-pregnatriene-3,20- dione. At the first suspected heat after injection, the heifers were examined by rectal palpation for condition of the uterus. Five to ten days later, they were again rectally palpated for signs of a new corpus luteum, which indicates a recent ovulation.

Determination of heat was made by two daily checks for mounting behavior and rupture of heat mount indicators.

Weights were determined initially and at 20-day intervals, except for the last weighing at 150 days which came after a 30-day interval. Each weighing was based on an average of three weighings on three consecutive days to account for fluctuation in fill.

Individual body weights for the entire experiments are presented in Table I. Table II contains the average daily weight gain (ADG) for each treatment group calculated from day zero for each time interval. Brackets in Table II approximate the mean interval of time during which the heifers in each group showed no estrous activity.

It is obvious from the data of Tables I and II that a 200 mg. injection for the test compound caused a substantial increase in rate of body weight gain throughout the 150 days of this experiment. The mg. and 100 mg. levels appeared to produce some increases in ADG during periods when estrus activity was inhibited; however, at all subsequent intervals, the ADG of the 50 mg. treated group was very similar to controls. At days the ADG showed a significant linear increase (P 0.05) with the 100 mg. and 200 mg. levels of test compound. At and days the increases in ADG were still in proportion to the levels of test compound, but after days on experiment, the over-all ADG from the 100 mg. and 200 mg. levels was significantly greater than controls (P 0.05) and the difference between these levels approached significance at the Pi=0.05 level. By the end of the experiment days), only the 200 mg. level produced an ADG which was significantly greater than control (approaching P=0.0l). Table II also suggests that the beneficial effect from the 100 mg. and 200 mg. levels of test compound on weight gain persited well past the first appearance of estrous behavior in each group.

TABLE I Body Weights Org.) 1

Post-treatment of- Level Heifer 0 20 40 60 80 100 130 (mg.) number days days days days days days days days Treatment:

148 347 358 375 386 387 397 412 421 141 410 421 429 441 445 455 474 482 Comm 0 164 363 374 388 401 414 418 423 433 Mean 374 386 397 410 415 166 381 396 410 417 419 136 394 404 413 424 426 9a, 115, 2l-trichloro-16a, 17a-(isopropylidcnedioxy)-1,4,6-pregna- 50 M91182 20mm 207 391 409 419 432 445 112 360 376 378 383 396 Mean 373 388 395 406 414 101 362 378 386 404 406 165 389 405 418 418 433 9a, 1lfi 21-tricl 1lor0-16a.- 17a-(isopropylidenedioxy)-1,4,6-pregna- 100 mdme 203 352 368 ass 392 404 143 428 443 449 464 477 Mean 375 392 403 412 422 105 393 406 430 437 447 208 362 380 392 400 402 9a, 116, 21-trich loro-16a, 1701-(isopropylidenedioxy).1,4,G-pregna- 200 3g g3: 29g tricne-3, 20dione 204 410 442 449 460 466 138 383 418 422 422 430 Mean.. 372 393 402 412 421 Mean of three consecutive days to account for fluctuation in fill. 2 Animal had hoof-rot at time of weighing, at 150 days, which apparently depressed its final weight.

TABLE II Average Daily Weight Gains (kg.)

Post-treatment of- Level 20 40 Test compound is 90.,11,3,21-trichloro-l611,17a-(isopropylidenedioxy)-1,4,6-pregnetrlene 3,20-d1one.

Brackets indicate approximate periods when all six heifers were not cycling.

EXAMPLE 2 Following the procedure of Example 1, beef heifers, approximately months of 'age, are given injections of 5 ml. of sesame oil containing 100 mg. or 200 mg. of 6,9a,115,21-tetrachl0ro-160:,170; (isopropylidenedioxy)- 1,4,6-pregnatriene-3,QO-dione or 911,11 5,21 trichloro 6- fluoro 16a,17a (isopropylidenedioxy) 1,4,6 pregnatriene-3,20-dione. The animals are weighed at the start of the treatment and at the intervals indicated in Example 1. Due to the inherent antifertility activity of these drugs, the animals show approximately the same mean interval times during which estrous activity is inhibited as those obtained with equivalent levels of 9a,11,B,21-trichloro- 16a,17a-(isopropylidenedioxy)-1,4,6 pregnatriene 3,20- dione. They also show growth responses for equivalent levels of drug.

What is claimed is:

1. A method for enhancing the growth rate of female ruminant animals comprising parenterally administering to said animals in a pharmaceutically acceptable carrier from about 100 mg. to 600 mg. of a steroid of the formula:

wherein R is a member selected from the group consisting of chlorine and fluorine.

2. A method according to claim 1 wherein the ruminant animals are cattle and the steroid is administered at from 200 mg. to 400 mg.

3. A method according to claim 1 wherein said steroid is administered in a single dose by intramuscular or subcutaneous injection.

4. A method according to claim 3 wherein the steroid is administered at from 200 mg. to 400 mg.

CHzCl wherein R is a member selected from the group consisting of chlorine and fluorine.

8. A method according to claim 7 wherein the steroid is 6,9a,11,8,21-tetrachloro-l6u,17a-(isopropylidenedioxy)- l,4,6-pregnatriene-3,20-dione.

9. A method according to claim 7 wherein the steroid is 9a,11{3,21 trichloro-6-fiuoro-16a,17a-(isopropylidenedioxy)-1,4,6-pregnatriene3,20-dione.

References Cited UNITED STATES PATENTS 3,608,076 9/1971 Heller 424241 3,541,086 11/1970 Fried 260-23455 3,211,727 10/1965 Heller et a1. 260--239.55 3,651,227 3/ 1972 Sickles 424238 3,036,917 5/1962 Harrop 424-240 3,417,182 12/1968 Babcock et al. 424243 3,639,585 2/1972 Hosse 424240 X 3,499,445 3/ 1970 Reed 128260 3,565,991 2/ 1971 Short 424-243 SHEP K. ROSE, Primary Examiner